HUE028345T2 - Stable preparations containing sulfonamides during storage - Google Patents

Stable preparations containing sulfonamides during storage Download PDF

Info

Publication number: HUE028345T2
Authority: HU; Hungary
Prior art keywords: water; group; solid; dispersible; plants
Prior art date: 2005-09-08

Application number

HUE06777111A

Other languages

English (en)

Hungarian (hu)

Inventor

Gerhard Schnabel

Hans-Peter Krause

Ralph Grohs

Original Assignee

Bayer Ip Gmbh

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2005-09-08

Filing date

2006-08-29

Publication date

2016-12-28

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35004164&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HUE028345(T2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2006-08-29 Application filed by Bayer Ip Gmbh filed Critical Bayer Ip Gmbh

2016-12-28 Publication of HUE028345T2 publication Critical patent/HUE028345T2/en

Links

239000000203 mixture Substances 0.000 title claims description 77
238000009472 formulation Methods 0.000 title claims description 38
229940124530 sulfonamide Drugs 0.000 title description 12
150000003456 sulfonamides Chemical class 0.000 title description 11
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239000002253 acid Substances 0.000 claims description 27
239000007787 solid Substances 0.000 claims description 22
238000000034 method Methods 0.000 claims description 17
150000003839 salts Chemical class 0.000 claims description 14
239000003795 chemical substances by application Substances 0.000 claims description 12
230000002363 herbicidal effect Effects 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
238000002360 preparation method Methods 0.000 claims description 11
125000003118 aryl group Chemical group 0.000 claims description 10
239000002270 dispersing agent Substances 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 7
239000003995 emulsifying agent Substances 0.000 claims description 6
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
239000002131 composite material Substances 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
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102100029469 WD repeat and HMG-box DNA-binding protein 1 Human genes 0.000 description 1
101710097421 WD repeat and HMG-box DNA-binding protein 1 Proteins 0.000 description 1
241001233305 Xanthisma Species 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
125000005133 alkynyloxy group Chemical group 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000000729 antidote Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
235000009052 artemisia Nutrition 0.000 description 1
238000012550 audit Methods 0.000 description 1
150000001540 azides Chemical class 0.000 description 1
FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
230000031018 biological processes and functions Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000011109 contamination Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
XXWNKVBJDWSYBN-UHFFFAOYSA-N diethoxy-phenoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CC=CC=C1 XXWNKVBJDWSYBN-UHFFFAOYSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000009477 fluid bed granulation Methods 0.000 description 1
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 description 1
238000005755 formation reaction Methods 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000003673 groundwater Substances 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
125000000262 haloalkenyl group Chemical group 0.000 description 1
125000004438 haloalkoxy group Chemical group 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
125000001072 heteroaryl group Chemical group 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 description 1
230000007774 longterm Effects 0.000 description 1
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 description 1
244000005700 microbiome Species 0.000 description 1
238000002156 mixing Methods 0.000 description 1
235000019426 modified starch Nutrition 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
230000035772 mutation Effects 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
LARRNBYMHFLZKK-UHFFFAOYSA-N pent-3-enamide Chemical compound CC=CCC(N)=O LARRNBYMHFLZKK-UHFFFAOYSA-N 0.000 description 1
125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
125000003367 polycyclic group Chemical group 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000010188 recombinant method Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
229940080237 sodium caseinate Drugs 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000707 stereoselective effect Effects 0.000 description 1
230000036435 stunted growth Effects 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
125000003107 substituted aryl group Chemical group 0.000 description 1
150000003455 sulfinic acids Chemical class 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
229910052645 tectosilicate Inorganic materials 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000004562 water dispersible granule Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

HUE06777111A 2005-09-08 2006-08-29 Stable preparations containing sulfonamides during storage HUE028345T2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP05019531		2005-09-08

Publications (1)

Publication Number	Publication Date
HUE028345T2 true HUE028345T2 (en)	2016-12-28

Family

ID=35004164

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HUE06777111A HUE028345T2 (en)	2005-09-08	2006-08-29	Stable preparations containing sulfonamides during storage

Country Status (21)

Country	Link
US (1)	US8158557B2 (pt)
EP (1)	EP1926378B1 (pt)
CN (3)	CN101262770A (pt)
AR (1)	AR055415A1 (pt)
AU (1)	AU2006289339B2 (pt)
BR (1)	BRPI0615902B1 (pt)
CA (1)	CA2622063C (pt)
CY (1)	CY1118146T1 (pt)
DK (1)	DK1926378T3 (pt)
EA (1)	EA013129B1 (pt)
ES (1)	ES2588165T3 (pt)
HU (1)	HUE028345T2 (pt)
IL (1)	IL189885A (pt)
LT (1)	LT1926378T (pt)
MX (1)	MX2008003356A (pt)
PL (1)	PL1926378T3 (pt)
PT (1)	PT1926378T (pt)
SI (1)	SI1926378T1 (pt)
UA (1)	UA90016C2 (pt)
WO (1)	WO2007028529A1 (pt)
ZA (1)	ZA200801430B (pt)

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EP1836894A1 (de) *	2006-03-25	2007-09-26	Bayer CropScience GmbH	Neue Sulfonamid-haltige feste Formulungen
EP1947946A2 (de) *	2005-09-08	2008-07-30	Bayer Cropscience Ag	Neue sulfonamid-haltige feste formulierungen
WO2007033759A1 (de) *	2005-09-16	2007-03-29	Bayer Cropscience Ag	Festformulierung
US9357747B1 (en) *	2007-08-17	2016-06-07	Ourpet's Company	Switchgrass cat litter
WO2010135350A2 (en) *	2009-05-20	2010-11-25	Pharmacopeia, Llc	Biphenyl intermediate compounds and methods for the preparation of a dual angiotensin ii and endothelin a receptor antagonist
AR081621A1 (es) *	2010-02-04	2012-10-10	Bayer Cropscience Ag	Procedimiento para la produccion de formulaciones estables de materiales solidos de sulfonamidas
CN103960234B (zh) *	2013-01-29	2016-12-28	粟贵武	磺酰脲类除草剂的新型稳定剂
CN103951655B (zh) *	2014-05-15	2016-05-11	天津市华宇农药有限公司	烟嘧磺隆衍生物和含该衍生物的除草剂、及其制备方法与应用
US9872498B2 (en) *	2015-02-12	2018-01-23	Rotam Agrochem International Company Limited	Process for preparing a novel formulation of rimsulfuron and use of the same
US20220132854A1 (en)	2019-02-19	2022-05-05	Gowan Company, L.L.C.	Stable liquid compositions and methods of using the same

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DK163123C (da)	1978-05-30	1992-06-09	Du Pont	Benzensulfonylurinstoffer til anvendelse som herbicider eller plantevaekstregulatorer, praeparat indeholdende dem samt deres anvendelse
ZA806970B (en)	1979-11-30	1982-06-30	Du Pont	Agricultural sulfonamides
JPS6284004A (ja)	1985-10-09	1987-04-17	Kumiai Chem Ind Co Ltd	改良された除草粒剤組成物
US5057144A (en) *	1988-05-09	1991-10-15	Bayer Aktiengesellschaft	Sulphonylaminocarbonyltriazolinones
US5534486A (en) *	1991-04-04	1996-07-09	Bayer Aktiengesellschaft	Herbicidal sulphonylaminocarbonyl triazolinones having substituents bonded via oxygen
DE19534910A1 (de)	1995-09-20	1997-03-27	Basf Ag	Herbizide Mischungen mit synergistischer Wirkung
US5830827A (en) *	1995-09-21	1998-11-03	Ishihara Sangyo Kaisha, Ltd.	Granular herbicidal composition comprising flazasulfuron and a sulfosuccinate or benzoate stabilizer
CN1158694A (zh) *	1996-11-25	1997-09-10	浙江乐吉化工厂	水稻田一次性投放型除草片剂
BRPI9807183B1 (pt) *	1997-02-05	2015-10-20	Basf Ag	mistura sólida, e, processos para a preparação de formulações herbicidas
CN1061215C (zh) *	1998-06-20	2001-01-31	吴应多	用于稻田的复配型除草剂
CN1287782A (zh) *	1999-09-14	2001-03-21	杭州振化化工有限公司	含丙草胺/苄嘧磺隆的除草剂组合物
TWI243019B (en) *	2000-08-31	2005-11-11	Basf Ag	Process for the preparation of a solid herbicidal formulation
DE10146590A1 (de) *	2001-09-21	2003-04-10	Bayer Cropscience Ag	Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern
AU2002333882A1 (en) *	2001-09-27	2003-04-14	Syngenta Participations Ag	Herbicidal composition
DE10307078A1 (de) *	2003-02-19	2004-09-09	Bayer Cropscience Gmbh	Verfahren zur Herstellung von wasserdispergierbaren Granulaten
CN1255029C (zh) *	2003-12-18	2006-05-10	浙江省农业科学院	草坪除草剂
EP1947946A2 (de) *	2005-09-08	2008-07-30	Bayer Cropscience Ag	Neue sulfonamid-haltige feste formulierungen
AR081621A1 (es) *	2010-02-04	2012-10-10	Bayer Cropscience Ag	Procedimiento para la produccion de formulaciones estables de materiales solidos de sulfonamidas

2006
- 2006-08-24 CN CNA2006800330448A patent/CN101262770A/zh active Pending
- 2006-08-24 CN CNA2006800331633A patent/CN101262772A/zh active Pending
- 2006-08-29 CA CA2622063A patent/CA2622063C/en active Active
- 2006-08-29 WO PCT/EP2006/008447 patent/WO2007028529A1/de not_active Ceased
- 2006-08-29 BR BRPI0615902A patent/BRPI0615902B1/pt active IP Right Grant
- 2006-08-29 AU AU2006289339A patent/AU2006289339B2/en active Active
- 2006-08-29 DK DK06777111.3T patent/DK1926378T3/en active
- 2006-08-29 MX MX2008003356A patent/MX2008003356A/es active IP Right Grant
- 2006-08-29 SI SI200632092A patent/SI1926378T1/sl unknown
- 2006-08-29 PT PT67771113T patent/PT1926378T/pt unknown
- 2006-08-29 CN CN200680033194.9A patent/CN101262769B/zh active Active
- 2006-08-29 EP EP06777111.3A patent/EP1926378B1/de active Active
- 2006-08-29 UA UAA200804469A patent/UA90016C2/ru unknown
- 2006-08-29 PL PL06777111.3T patent/PL1926378T3/pl unknown
- 2006-08-29 EA EA200800752A patent/EA013129B1/ru not_active IP Right Cessation
- 2006-08-29 LT LTEP06777111.3T patent/LT1926378T/lt unknown
- 2006-08-29 ES ES06777111.3T patent/ES2588165T3/es active Active
- 2006-08-29 HU HUE06777111A patent/HUE028345T2/en unknown
- 2006-09-06 AR ARP060103879A patent/AR055415A1/es active IP Right Grant
- 2006-09-08 US US11/517,458 patent/US8158557B2/en active Active
2008
- 2008-02-12 ZA ZA200801430A patent/ZA200801430B/xx unknown
- 2008-03-02 IL IL189885A patent/IL189885A/en active IP Right Grant
2016
- 2016-08-24 CY CY20161100836T patent/CY1118146T1/el unknown

Also Published As

Publication number	Publication date
CN101262770A (zh)	2008-09-10
EP1926378A1 (de)	2008-06-04
SI1926378T1 (sl)	2016-10-28
PL1926378T3 (pl)	2016-11-30
US8158557B2 (en)	2012-04-17
UA90016C2 (ru)	2010-03-25
CA2622063C (en)	2014-04-22
BRPI0615902B1 (pt)	2016-04-12
AU2006289339B2 (en)	2013-04-04
IL189885A (en)	2016-03-31
LT1926378T (lt)	2016-09-12
CN101262772A (zh)	2008-09-10
AR055415A1 (es)	2007-08-22
US20070054807A1 (en)	2007-03-08
IL189885A0 (en)	2008-08-07
EA200800752A1 (ru)	2008-08-29
ZA200801430B (en)	2008-12-31
EA013129B1 (ru)	2010-02-26
CY1118146T1 (el)	2017-06-28
CN101262769A (zh)	2008-09-10
AU2006289339A1 (en)	2007-03-15
PT1926378T (pt)	2016-08-30
EP1926378B1 (de)	2016-06-29
ES2588165T3 (es)	2016-10-31
CN101262769B (zh)	2014-06-18
WO2007028529A1 (de)	2007-03-15
MX2008003356A (es)	2008-03-25
BRPI0615902A2 (pt)	2011-05-31
DK1926378T3 (en)	2016-09-12
CA2622063A1 (en)	2007-03-15

Publication	Publication Date	Title
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FI82877C (fi)	1991-05-10	Herbicida blandningar baserade pao foereningen av typen n-(fosfonometylglysyl)-sulfonylamin.
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